CN105951119B - A kind of method for preparing sodium hydroxide - Google Patents

A kind of method for preparing sodium hydroxide Download PDF

Info

Publication number
CN105951119B
CN105951119B CN201610515916.XA CN201610515916A CN105951119B CN 105951119 B CN105951119 B CN 105951119B CN 201610515916 A CN201610515916 A CN 201610515916A CN 105951119 B CN105951119 B CN 105951119B
Authority
CN
China
Prior art keywords
cathode chamber
chamber
sodium hydroxide
anode chamber
cathode
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201610515916.XA
Other languages
Chinese (zh)
Other versions
CN105951119A (en
Inventor
杜旭华
龚玮
谢毅龙
张威
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang Zhenyang Development Co., Ltd
Original Assignee
NINGBO OCEANKING CHEMICAL DEVELOPMENT Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NINGBO OCEANKING CHEMICAL DEVELOPMENT Co Ltd filed Critical NINGBO OCEANKING CHEMICAL DEVELOPMENT Co Ltd
Priority to CN201610515916.XA priority Critical patent/CN105951119B/en
Publication of CN105951119A publication Critical patent/CN105951119A/en
Application granted granted Critical
Publication of CN105951119B publication Critical patent/CN105951119B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • Y02P20/129Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Inorganic Chemistry (AREA)
  • Automation & Control Theory (AREA)

Abstract

A kind of method for preparing sodium hydroxide, includes the following steps, S1, refined saturated nacl aqueous solution is added in preheater preheats, preheating temperature is 47 DEG C~63 DEG C;S2, the saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, open power supply be powered, when the electric current of circuit reaches 5.3KA, into anode chamber add in acid, and keep cathode chamber pH value be 2~3;S3, the temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction;S4, pumping process is carried out to cathode chamber and anode chamber, and it is 47.35 × 10 to keep the pressure of cathode chamber and anode chamber3Pa~53.41 × 103Pa;S5, the sodium hydroxide solution that cathode chamber side generates is partly refluxed in cathode chamber, output hydrogen above the electrode of cathode chamber, output chlorine above the electrode of anode chamber.This kind is electrolysed the mode of saturation sodium chlorate, reduces attachment of the gas in electrode surface, improves the conductive capability of entire electrolysis system, so as to substantially increase the yield of sodium hydroxide.

Description

A kind of method for preparing sodium hydroxide
Technical field
The present invention relates to the preparation of industrial chemicals, more particularly to a kind of method for preparing sodium hydroxide.
Background technology
Sodium hydroxide, chemical formula NaOH are commonly called as caustic soda, caustic soda, caustic soda, are a kind of highly basic with strong corrosive, Generally sheet or particle shape, it is soluble easily in water(Heat release when being dissolved in water)And alkaline solution is formed, separately there is hygroscopy, easily draw empty Vapor in gas(Deliquescence)And carbon dioxide(It is rotten), hydrochloric acid can be added in and check whether to go bad.
In the prior art, the mode of production of industrial sodium hydroxide is main mainly to be electrolysed based on saturated salt solution In chlorine industry with first the present.
But at the same time, due to when saturation table salt water is electrolysed, hydroxide ion that cathode chamber generates can be by On the cation-exchange membrane for gradually gathering cathode chamber side, as concentration of the hydroxyl at this constantly increases, so as to just It is possible that cation-exchange membrane is crossed, so as to will result in the problems such as anode chamber's chlorine yield falls sharply.
Invention content
The purpose of the present invention is to provide a kind of methods for preparing sodium hydroxide for helping to improve naoh concentration.
The present invention above-mentioned purpose technical scheme is that:A kind of method for preparing sodium hydroxide, Include the following steps,
S1, it refined saturated nacl aqueous solution is added in preheater preheats, preheating temperature is 47 DEG C~63 DEG C;
S2, the saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, and cathode chamber is then passed through distilled water, And open power supply energization, when the electric current of circuit reaches 5.3KA, into anode chamber add in acid, and keep cathode chamber pH value be 2 ~3;
S3, the temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction;
S4, pumping process is carried out to cathode chamber and anode chamber, and keep the pressure of cathode chamber and anode chamber for 47.35 × 103Pa~53.41 × 103Pa;
S5, the sodium hydroxide solution that cathode chamber side generates is partly refluxed in cathode chamber, the electrode of cathode chamber Top output hydrogen, the electrode top output chlorine of anode chamber.
By the above method, it is to preheat refined saturated sodium-chloride first, can causes saturated sodium-chloride in this way It can be rapidly electrolysed after entering electrolytic cell, improve the efficiency of electrolysis.
Secondly, by way of acid adding in the anode compartment, the pH value of solution is improved, cathode chamber can be effectively prevented in this way The hydroxyl low amounts of generation penetrates cation-exchange membrane, and causes the absorption to chlorine in anode chamber, so as to not only reduce chlorine The yield of gas, meanwhile, it is also introduced into new substance.
Since the saturated vapor pressure of the water at 70 DEG C is 31.18 × 103The pressure of electrolytic cell is adjusted to by Pa 47.35×103Pa~53.41 × 103Pa can effectively improve the efficiency that hydrogen and chlorine are detached from solution in this way, So as to be conducive to improve the normal output of hydrogen and chlorine, and can also reduce in chlorine back dissolving to saturated nacl aqueous solution Amount, and it is also beneficial to improve the amount of sodium hydroxide output.
By the way that in the sodium hydroxide partial reflux to cathode chamber by output, the dense of sodium hydroxide can be effectively improved in this way Degree, the size of concentration can be controlled by regurgitant volume, and in the naoh concentration for increasing cathode chamber, be also improved whole The conductive capability of a electrolytic cell, so as to be conducive to improve the yield of sodium hydroxide.
Preferably, the hydrogen portion of S5 outputs is passed into along the surface of cation-exchange membrane in cathode chamber.
Preferably, the amount for passing through the hydrogen in cathode chamber is generate hydrogen total amount 30%~40%.
Being passed into cathode chamber along the surface of cation-exchange membrane by hydrogen in this way, can be effectively to cation The solution of other parts exchanged in the solution and cathode chamber of film surface causes turbulent flow, so as to advantageously reduce hydroxyl sun from The surface aggregation of proton exchange, and then also can further reduce the possibility that hydroxyl penetrates cation-exchange membrane.
It is stirred preferably, opening agitating paddle in S3 in the cathodic compartment, the rotating speed of agitating paddle is 60~70 turns/min.
Due to can be attached on cathode in the form of bubble after hydrionic generation, so as to be generated on the surface of cathode One layer of air film, can thus reduce the area that cathode is contacted with the aqueous slkali of solution, so as to result under aqueous slkali electric conduction quantity Drop, and then it is unfavorable for the generation of sodium hydroxide.By way of stirring, the stream of sodium hydroxide in cathode chamber can be effectively improved Momentum is attached to so as to eliminate hydrogen on cathode, improves the efficiency of hydrogen generation.
And the rotating speed of 60~70 turns/min can ensure that the flow velocity of the sodium hydroxide solution in cathode chamber is unlikely to excessive, from And cation-exchange membrane is impacted.
Preferably, the regurgitant volume of sodium hydroxide solution is the 1/5~3/5 of its total yield output.
It is stirred preferably, opening agitating paddle in S3 in the anode compartment, the rotating speed of agitating paddle is 40~45 turns/min.
Saturated nacl aqueous solution in anode chamber is stirred, is mainly attached on anode also for reduction chlorine, And while 40~45 turns/min rotating speeds can ensure that chlorine bubbles are normally detached from anode, chlorine bubbles itself can also be avoided It ruptures and is dissolved in saturated nacl aqueous solution again.
Preferably, the acid added in S2 is hydrochloric acid.
Hydrochloric acid can not only effectively improve the hydrionic concentration of anode chamber, meanwhile, it will not be dense by new ion Degree introduces, in this way can be to avoid influence of the other impurities to the purity of chlorine and the conductive capability of saturated nacl aqueous solution.
In conclusion the invention has the advantages that:
1. by reducing the pressure in electrolytic cell, the concentration of superjacent hydrogen and chlorine can be efficiently reduced, so as to Be conducive to the output of hydrogen and chlorine, and then be also advantageous for improving the yield of sodium hydroxide;
2. by way of stirring, the attachment of hydrogen and chlorine on the electrode is eliminated, so as to substantially increase entire electricity The electric conductivity of slot is solved, and then is conducive to improve the yield of sodium hydroxide.
3. the pH value of solution in anode chamber can not only be controlled by adding in hydrochloric acid, while new impurity member will not be introduced Element.
Specific embodiment
Embodiment 1,
By refined saturated nacl aqueous solution using flow as 200m3/ h is added in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, is added with the flow of 300 m3/h Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 1/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 30% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/h, mass concentration 34%, the production of sodium hydroxide Rate is 97.5%.
Embodiment 2,
Refined saturated nacl aqueous solution using flow is added to as 200m3/h in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, is added with the flow of 300 m3/h Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 3/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 40% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/h, mass concentration 41%, the production of sodium hydroxide Rate is 98.6%.
Embodiment 3,
Refined saturated nacl aqueous solution using flow is added to as 200m3/h in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, is added with the flow of 300 m3/h Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 2/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 35% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/h, mass concentration 36%, the production of sodium hydroxide Rate is 97.9%.
Embodiment 4,
Refined saturated nacl aqueous solution using flow is added to as 200m3/h in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, with 300 m3The flow of/h adds Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 1/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 35% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/ h, mass concentration 35%, the production of sodium hydroxide Rate is 97.8%.
Embodiment 5,
By refined saturated nacl aqueous solution using flow as 200m3/ h is added in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, is added with the flow of 300 m3/h Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 1/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 40% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/ h, mass concentration 35.5%, sodium hydroxide Yield is 98.1%.
Embodiment 6,
By refined saturated nacl aqueous solution using flow as 200m3/ h is added in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, is added with the flow of 300 m3/h Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 2/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 40% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/h, mass concentration 37%, the production of sodium hydroxide Rate is 98.0%.
Embodiment 7,
Refined saturated nacl aqueous solution using flow is added to as 200m3/h in preheater and is preheated, preheating temperature It is 47 DEG C~63 DEG C;Saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, is added with the flow of 300 m3/h Enter into electric tank cathode room, and open power supply energization, when the electric current of circuit reaches 5.3KA, hydrochloric acid is added in into anode chamber, And keep cathode chamber pH value be 2~3;The temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction, together When, the speed of agitator of cathode chamber is 60~70 turns/min, and the speed of agitator of anode chamber is 40~45 turns/min;To cathode chamber and sun Pole room carries out pumping process, and it is 47.35 × 103Pa~53.41 × 103Pa to keep the pressure of cathode chamber and anode chamber;Cathode Output hydrogen above the electrode of room, the electrode top output chlorine of anode chamber, is collected into hydrogen gas tank and chlorine pot respectively, will be cloudy The 3/5 of the sodium hydroxide solution that pole room side generates is back in cathode chamber, the hydrogen total amount that will be generated above cathode chamber 30% flow back into cathode chamber.It is final produce the amount of sodium hydroxide is 100m3/ h, mass concentration 40%, the production of sodium hydroxide Rate is 98.4.
This specific embodiment is only explanation of the invention, is not limitation of the present invention, people in the art Member can as needed make the present embodiment the modification of no creative contribution after this specification is read, but as long as at this It is all protected in the right of invention by Patent Law.

Claims (3)

1. a kind of method for preparing sodium hydroxide, includes the following steps,
S1, it refined saturated nacl aqueous solution is added in preheater preheats, preheating temperature is 47 DEG C~63 DEG C;
S2, the saturated nacl aqueous solution after preheating is transferred in electrolyzer anode chamber, and cathode chamber is then passed through distilled water, and beats Switch power supply be powered, when the electric current of circuit reaches 5.3KA, into anode chamber add in acid, and keep cathode chamber pH value be 2~3;
S3, the temperature of electrolytic cell is increased to 62 DEG C~73 DEG C, and carries out heat preservation energization reaction;
S4, pumping process is carried out to cathode chamber and anode chamber, and it is 47.35 × 10 to keep the pressure of cathode chamber and anode chamber3Pa~ 53.41×103Pa;
S5, the sodium hydroxide solution that cathode chamber side generates is partly refluxed in cathode chamber, above the electrode of cathode chamber Output hydrogen, the electrode top output chlorine of anode chamber;
Wherein, the hydrogen portion of S5 outputs is passed into along the surface of cation-exchange membrane in cathode chamber, by cathode chamber The amount of hydrogen be to open agitating paddle in the cathodic compartment in 30%~40%, the S3 for generate hydrogen total amount and be stirred, agitating paddle Rotating speed is 60~70 turns/min, and the regurgitant volume of sodium hydroxide solution is the 1/5~3/5 of its total yield output.
2. a kind of method for preparing sodium hydroxide according to claim 1, it is characterised in that:It is opened in the anode compartment in S3 Agitating paddle is stirred, and the rotating speed of agitating paddle is 40~45 turns/min.
3. a kind of method for preparing sodium hydroxide according to claim 1, it is characterised in that:The acid added in S2 is salt Acid.
CN201610515916.XA 2016-07-04 2016-07-04 A kind of method for preparing sodium hydroxide Active CN105951119B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610515916.XA CN105951119B (en) 2016-07-04 2016-07-04 A kind of method for preparing sodium hydroxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610515916.XA CN105951119B (en) 2016-07-04 2016-07-04 A kind of method for preparing sodium hydroxide

Publications (2)

Publication Number Publication Date
CN105951119A CN105951119A (en) 2016-09-21
CN105951119B true CN105951119B (en) 2018-07-06

Family

ID=56902366

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610515916.XA Active CN105951119B (en) 2016-07-04 2016-07-04 A kind of method for preparing sodium hydroxide

Country Status (1)

Country Link
CN (1) CN105951119B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109208024B (en) * 2018-09-21 2020-02-28 宁波镇洋化工发展有限公司 Chlor-alkali production process
CN110923077A (en) * 2019-11-21 2020-03-27 甘肃农业职业技术学院 Preparation method of pine phytoncide process soap
CN112125978A (en) * 2020-09-16 2020-12-25 陕西国防工业职业技术学院 Preparation method of high-viscosity water-soluble cellulose ether
CN115198108B (en) * 2021-04-13 2024-03-29 浙江新化化工股份有限公司 Method for extracting lithium

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0445295A (en) * 1990-06-12 1992-02-14 Toagosei Chem Ind Co Ltd Method for removing chlorate in brine
JPH1161476A (en) * 1997-08-22 1999-03-05 Chlorine Eng Corp Ltd Starting operation of electrolytic bath in ion-exchange membrane electrolytic process
CN103305864A (en) * 2012-03-15 2013-09-18 拜耳知识产权有限责任公司 Method for the electrolysis of alkali chlorides with oxygen consumption electrodes in a micro-gap arrangement
CN204097575U (en) * 2013-11-20 2015-01-14 新疆宜化化工有限公司 Electrolysis cells in ionic exchange membrane caustic
CN104532283A (en) * 2014-12-17 2015-04-22 济宁金威煤电有限公司 Method and device for producing caustic soda through electrolysis by replacing part of fine brine with light salt brine
CN105154910A (en) * 2015-09-21 2015-12-16 宁波镇洋化工发展有限公司 Process for producing alkali

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0445295A (en) * 1990-06-12 1992-02-14 Toagosei Chem Ind Co Ltd Method for removing chlorate in brine
JPH1161476A (en) * 1997-08-22 1999-03-05 Chlorine Eng Corp Ltd Starting operation of electrolytic bath in ion-exchange membrane electrolytic process
CN103305864A (en) * 2012-03-15 2013-09-18 拜耳知识产权有限责任公司 Method for the electrolysis of alkali chlorides with oxygen consumption electrodes in a micro-gap arrangement
CN204097575U (en) * 2013-11-20 2015-01-14 新疆宜化化工有限公司 Electrolysis cells in ionic exchange membrane caustic
CN104532283A (en) * 2014-12-17 2015-04-22 济宁金威煤电有限公司 Method and device for producing caustic soda through electrolysis by replacing part of fine brine with light salt brine
CN105154910A (en) * 2015-09-21 2015-12-16 宁波镇洋化工发展有限公司 Process for producing alkali

Also Published As

Publication number Publication date
CN105951119A (en) 2016-09-21

Similar Documents

Publication Publication Date Title
CN105951119B (en) A kind of method for preparing sodium hydroxide
CN104131311B (en) Mineralising CO2preparing sodium bicarbonate or sodium carbonate externally export the method for electric energy
AU2014203346B2 (en) A process for making lithium carbonate from lithium chloride
CN103882468B (en) A kind of electrolysis-bipolar membrane electrodialysis system and production method thereof of being produced lithium hydroxide by Quilonum Retard
CN110656343B (en) Method for preparing double-alkali co-production high-purity gypsum from mirabilite and limestone by utilizing PCET reaction
CN105603452B (en) Novel high-efficient hypochlorite generator
CN109772169A (en) A kind of bipolar membrane electrodialysis system and its method for preparing lithium hydroxide
CN104477950B (en) Dolomite passes through CO2The method of mineralising high purity basic magnesium carbonate and calcium carbonate
CN106801233A (en) A kind of electrolysis prepares the system and method for high-purity TPAOH
CN105154910B (en) A kind of production technology of alkali
RU2751710C2 (en) Method for producing high-purity lithium hydroxide monohydrate from materials containing lithium carbonate or lithium chloride
CN110395749A (en) A method of lithium chloride is prepared using the displacement reaction electrodialysis of four compartments
RU2157338C2 (en) Method of production of high-purity lithium hydroxide from natural brines
CN108570689A (en) Electrolysis prepares the device and method of chlorine dioxide
CN102134724B (en) Method for desalting waste liquor in sodium carbonate production by using anion-exchange membrane electrolyzer
CN1369576A (en) Reverse electrolyzer with dual membranes and three chambers
CN107022769B (en) A kind of method and device for extracting high-purity monohydrate lithium hydroxide from the material containing lithium carbonate
CN205115612U (en) Novel super -pure hydrogen generator
US20210047742A1 (en) Method of making alkali and gypsum by proton-coupled electron transfer reaction
CN112281180A (en) Method for preparing chlorine by electrolyzing concentrated seawater through bipolar membrane
CN113481521B (en) Continuous chlor-alkali industrial electrolysis alkali preparation device and method
CN106191912B (en) A method of preparing chlorine
CN109930168A (en) A kind of processing unit and processing method of hopcalite agent waste liquid sodium sulphate liquid
CN110029354A (en) Utilize the method for lithium chloride Direct Electrolysis preparation LITHIUM BATTERY lithium hydroxide
CN210458383U (en) Device suitable for inorganic salt electrolysis

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CP03 Change of name, title or address

Address after: 315204 No. 655 Haitian Road, Ningbo Petrochemical Economic Development Zone, Zhenhai District, Zhejiang, Ningbo, China

Patentee after: Zhejiang Zhenyang Development Co., Ltd

Address before: 315204 Chemical Industrial Zone, Zhejiang, Ningbo, China

Patentee before: NINGBO OCEANKING CHEMICAL DEVELOPMENT Co.,Ltd.

CP03 Change of name, title or address